abnormal gallbladder physiology Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A functional anomaly of the gallbladder. (Human Phenotype Ontology, HP_0012438)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012438
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8 genes associated with the abnormal gallbladder physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABCB4 ATP-binding cassette, sub-family B (MDR/TAP), member 4
ALDOA aldolase A, fructose-bisphosphate
ARSA arylsulfatase A
BPGM 2,3-bisphosphoglycerate mutase
GPI glucose-6-phosphate isomerase
HK1 hexokinase 1
PKLR pyruvate kinase, liver and RBC
TPI1 triosephosphate isomerase 1